BIOSINTESIS DE LA SEROTONINA PDF

Metabolismo de la 5-HT Figura 3. Biosíntesis y catabolismo de la 5-HT. es convertido por la monoamino oxidasa y aldehído deshidrogenasa. Biosintesis de Aminoacidos – Free download as Powerpoint Presentation .ppt /.pptx), Neurotransmisores: DOPA, DOPAMINA, serotonina, etc. Serotonina Estructura química. Biosíntesis Localización Bibliografía Fisiología Medica; William Ganong, 12a edición, Ed. Manual Moderno, pp.

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Epithelial, endothelial, and mast cells stained positive for serotonin transporters. We combined morphological and biochemical techniques to begin approaching these aspects of serotonin in the rat caput epididymis.

CDE; Semana 5, Serotonina by Alexis Onofre Luna on Prezi

Interestingly, serotonin concentration and tryptophan hydroxylase activity tended to be higher in breeding males than in those with no mating experience. La clinica comenzo a los 5 meses con temblor cefalico y de las extremidades superiores, en reposo e intencional, intermitente, que desaparecio en un mes. El deficit de la enzima trifosfato de guanosina ciclohidrolasa 1 GTPCH 1 origina una disminucion de la sintesis de la tetrahidrobiopterina BH4cofactor indispensable en la sintesis de la tirosina, la dopamina y la serotonina.

Hay que destacar en este caso la mejoria tan satisfactoria, tanto motora como cognitiva, tras iniciar el tratamiento sustitutivo, ya que el nivel cognitivo suele quedar afectado en muchos casos.

The caput epididymis of some mammals contains large quantities of serotonin whose origin, targets, and physiological variations have been poorly studied. Morphological and Biochemical Studies.

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Serotonina

Only epithelial cells showed tryptophan hydroxylase immunoreactivity; this enzyme catalyzes the limiting step in the serotonin synthetic pathway.

The clinical features began at the age of 5 months with intermittent upper limb and brain tremors, both at rest and intentional, that disappeared after a month. The patient later presented psychomotor regression with loss of head control, diminished active movements, difficulty in bimanual manipulation, hypomimia and severe global hypotonia, which was the reason for the study of a progressive encephalopathy.

We report the case of a girl with autosomal recessive GTPCH deficiency, who was diagnosed at 14 months by means of an analysis of the cerebrospinal fluid with pterin, HVA and 5-HIAA deficiency, and positive phenylalanine overload test and genetic study.

It is an infrequent disease that produces psychomotor delay or regression and movement disorders, although treatment can improve or even correct the clinical signs and symptoms.

Psychomotor development was normal, mild axial hypotonia being found in the examination while the complementary tests that were performed were normal.

We think that these results support the existence of a local serotoninergic system in the rat caput epididymis that might regulate some aspects serotojina male reproductive function. Serotonin immunostaining was detected in mast, epithelial, and neuroendocrine cells. Endothelial and mast cells labeled positive for 5HT1B serotonin receptors and spermatozoa dde 5HT2A and 5HT3 serotonin receptor immunoreactivity.

Theanine-induced reduction of brain serotonin concentration in rats

Posteriormente presento regresion psicomotora con perdida del sosten cefalico, disminucion de los movimientos activos, dificultad para la manipulacion bimanual, hipomimia e hipotonia global grave, lo que motivo el estudio de una encefalopatia progresiva.

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Chromatographic analyses documented the presence of tryptophan hydroxylase in the caput, and showed that both its activity and serotonin availability increased with sexual maturation and decreased following p-chlorophenylalanine treatment, an inhibitor of tryptophan hydroxylase activity.

Today, the patient is 5 years old, has an adequate psychomotor development for her age, is in the third year of preschool education and has caught up with the level of the rest of her classmates. El desarrollo psicomotor era normal, destacaba una hipotonia axial leve en la exploracion y las pruebas complementarias realizadas fueron normales.

Es una enfermedad poco frecuente que produce un retraso o regresion psicomotora y trastornos del movimiento, y en la que el tratamiento puede mejorar o incluso corregir la clinica. In this case attention must be drawn to the extremely satisfactory motor and cognitive improvement of the patient after starting replacement therapy, as in many cases the cognitive level is usually affected on a permanent basis.

A deficiency of the enzyme guanosine triphosphate cyclohydrolase I GTPCH 1 causes a reduction in the synthesis of tetrahydrobiopterin BH4a cofactor that is essential in the synthesis of tyrosine, dopamine biosintdsis serotonin.